Relevant bibliographies by topics / Hydroxyle radical

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Hydroxyle radical'

Author: Grafiati
Published: 31 August 2024
Last updated: 31 July 2025

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Journal articles on the topic "Hydroxyle radical"

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Zylber, Jean, Nicole Zylber, Daniel Lefort, Christiane Ferradini, and Bernard Hickel. "Régiosélectivité de la réaction des radicaux hydroxyle et hydroxy-2 propyle-2 avec l'hypoxanthine." Canadian Journal of Chemistry 66, no. 2 (1988): 283–87. http://dx.doi.org/10.1139/v88-048.

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The reactivity of [Formula: see text] and (CH3)2ĊOH radicals with hypoxanthine was studied under comparable γ-irradiation conditions. A difference in regioselectivity of attack by the electrophilic [Formula: see text] radical and the nucleophilic (CH3)2ĊOH radical is observed, the latter leading in 70% yield to a C-8 substituted product. The rate constants of the addition of the radical to hypoxanthine were determined by pulse radiolysis to be k = 1.4 × 108 M−1 s−1 in acid medium, and in neutral medium k = 7 × 105 M−1 s−1. The much more reactive [Formula: see text] radical leads essentially to
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Gallard, H., J. De Laat, and B. Legube. "Étude comparative de la vitesse de décomposition de H2O2 et de l'atrazine par les systèmes Fe(III)/H2O2, Cu(II)/H2O2 et Fe(III)/Cu(II)/H2O2." Revue des sciences de l'eau 12, no. 4 (2005): 713–28. http://dx.doi.org/10.7202/705374ar.

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Cette étude a eu pour objectif de comparer les vitesses de décomposition du peroxyde d'hydrogène et d'oxydation de l'atrazine par les systèmes catalytiques Fe(III)/H2O2, Cu(II)/H2O2, et Fe(III)/Cu(II)/H2O2. Les expériences ont été réalisées à pH 3,0, à une température de 25,0 (± 0,2) °C, en milieu perchlorate, en présence et en absence d'oxygène dissous. L'étude comparative a confirmé que les vitesses de décomposition de H2O2 et d'oxydation de l'atrazine sont beaucoup plus lentes en présence de Cu(II) qu'en présence de Fe(III) et l'addition de Cu(II) augmente l'efficacité du système Fe(III)/H2
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Zheng, Cheng-Dong, Gang Li, Hu-Qiang Li, Xiao-Jing Xu, Jin-Ming Gao, and An-Ling Zhang. "DPPH-Scavenging Activities and Structure-Activity Relationships of Phenolic Compounds." Natural Product Communications 5, no. 11 (2010): 1934578X1000501. http://dx.doi.org/10.1177/1934578x1000501112.

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Thirty-eight phenolic compounds (including 31 flavonoids) were examined for their DPPH radical-scavenging activities, and structure-activity relationships were evaluated. Specifically, the presence of an Ortho-dihydroxyl structure in phenolics is largely responsible for their excellent antiradical activity. 3-Hydroxyl was also essential to generate a high radical-scavenging activity. An increasing number of hydroxyls on flavones with a 3′,4′-dihydroxyl basic structure, the presence of a third hydroxyl group at C-5′, a phloroglucinol structure, glycosylation and methylation of the hydroxyls, an
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Rhim, Tae-Jin, Hee-Sun Jeong, Young-Jin Kim, et al. "A study on the comparison of antioxidant effects among cultivated ginseng, and cultivated wild ginseng extracts -Using the measurement of superoxide and hydroxy radical scavenging activities-." Journal of Korean Institute of Herbal Acupuncture 12, no. 2 (2009): 7–12. http://dx.doi.org/10.3831/kpi.2009.12.2.007.

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Choi, Jeong-Hwan, Dong-Hun Shin, Hye-Bin Kim, Jong-Gook Kim, and Kitae Baek. "One-step Oxidation of Total Organic Carbon, Total Nitrogen, and Total Phosphorous using Wet Chemical Oxidation." Journal of Korean Society of Environmental Engineers 42, no. 12 (2020): 603–9. http://dx.doi.org/10.4491/ksee.2020.42.12.603.

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Objective:This study proposed the simultaneous multi-oxidation of total organic carbon, total nitrogen, and total phosphorous using modified wet chemical oxidation method.Methods:The multi oxidation process was based on the dual radical system with sulfate and hydroxyl radicals. The sodium persulfate (Na2S2O8) and sodium hydroxide (NaOH) were activated at 40℃ and UV irradiation with 254 nm to generate the sulfate radical and hydroxyl radical. The organic matters were oxidized by the dual radicals, and TOC, TN, and TP values were compared with the control group.Results and Discussion:The dual r
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Duwe, A. K., J. Werkmeister, J. C. Roder, R. Lauzon, and U. Payne. "Natural killer cell-mediated lysis involves an hydroxyl radical-dependent step." Journal of Immunology 134, no. 4 (1985): 2637–44. http://dx.doi.org/10.4049/jimmunol.134.4.2637.

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Abstract The role of oxygen radicals in lysis of K562 target cells by human natural killer (NK) cells was determined by addition of scavengers of these free radicals. Lysis was greatly reduced under hypoxic conditions. Superoxide dismutase and cytochrome c, scavengers of superoxide anions, and catalase and scavengers of hypochlorite had no effect on lysis. Of 15 hydroxyl radical scavengers tested, 13 inhibited lysis. These were not toxic, because cell morphology and spontaneous chromium release were not affected and preculture with scavengers was not inhibitory. These scavengers differed widel
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Vrecko, Karoline, and Gilbert Reibnegger. "Influence of 7,8 Dihydroneopterin and Hyperoxia on Neurite Growth and Tyrosine Hydroxylase Activity of PC 12 Cells." Pteridines 13, no. 3 (2002): 94–99. http://dx.doi.org/10.1515/pteridines.2002.13.3.94.

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Abstract The influence of dihydroneopterin on tyrosine hydroxylase activity in PC 12 cells was investigated under normoxic and hyperoxic conditions, and with or without iron ions in the incubation medium. Low dihydroneopterin concentrations as well as hyperoxia increase tyrosine hydroxylase activity. Due to a too vigorous radical formation, high dihydroneopterin concentrations lead to a decrease of tyrosine hydroxylation in normoxic state and even more strongly in hyperoxic state. Similar depression of tyrosine hydroxylase activity was seen after addition of iron ions, which can form hydroxyl
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Gebicka, L., and J. L. Gebicki. "Scavenging of oxygen radicals by heme peroxidases." Acta Biochimica Polonica 43, no. 4 (1996): 673–78. http://dx.doi.org/10.18388/abp.1996_4463.

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The reactions of two heme peroxidases, horseradish peroxidase and lactoperoxidase and their compounds II (oxoferryl heme intermediates, Fe(IV) = O or ferric protein radical Fe(III)R.) and compounds III (resonance hybrids [Fe(III)-O2-. Fe(II)-O2] with superoxide radical anion generated enzymatically or radiolytically, and with hydroxyl radicals generated radiolytically, were investigated. It is suggested that only the protein radical form of compound II of lactoperoxidase reacts with superoxide, whereas compound II of horseradish peroxidase, which exists only in oxoferryl form, is unreactive to
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Bi, Yong Guang, and Chun Chun Liu. "Study on Scavenging Free Radical Activity with Polysaccharides Materials in Chuanxiong Based on Composite Properties of Biomaterials." Advanced Materials Research 583 (October 2012): 244–47. http://dx.doi.org/10.4028/www.scientific.net/amr.583.244.

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By using spectrophotometric detection of the Chuanxiong polysaccharides on the free radical scavenging. The results show that the Chuanxiong polysaccharides on DPPH radical, hydroxyl radical (HO•) and superoxide anion radical (•) clearance. Scavenging ability with the the Chuanxiong polysaccharide concentration increased, and showed the dose-effect relationship. Concentration of 2.0mg/mL when DPPH radicals clear the rate of 35.61%, while the rate of hydroxyl radicals and superoxide anion radical scavenging, clear the rate of 57.78% and 57.14%. Chuanxiong polysaccharide is an ideal natural anti
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Flitter, W. D., and R. P. Mason. "The spin trapping of pyrimidine nucleotide free radicals in a Fenton system." Biochemical Journal 261, no. 3 (1989): 831–39. http://dx.doi.org/10.1042/bj2610831.

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The reaction of the hydroxyl radical, generated by a Fenton system, with pyrimidine deoxyribonucleotides was investigated by using the e.s.r. technique of spin trapping. The spin trap t-nitrosobutane was employed to trap secondary radicals formed by the reaction of the hydroxyl radical with these nucleotides. The results presented here show that hydroxyl-radical attack on thymidine, 2-deoxycytidine 5-monophosphate and 2-deoxyuridine 5-monophosphate produced nucleotide-derived free radicals. The results indicate that .OH radical attack occurs predominantly at the carbon-carbon double bond of th
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Dissertations / Theses on the topic "Hydroxyle radical"

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Alkhuraiji, Turki. "Ionisation par faisceau d'électrons de solutions aqueuses de benzènesulfonate et naphthalènesulfonate et sous-produits." Thesis, Poitiers, 2013. http://www.theses.fr/2013POIT2259/document.

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Ce sujet entre dans le cadre de l'étude d'un procédé d'oxydation avancé innovant dans le domaine de la dépollution des eaux, à savoir l'ionisation par faisceau d'électrons. Le radical hydroxyle (•OH) et l'électron hydraté (e−aq) sont les deux espèces majoritaires issues de l'ionisation de solutions aqueuses par un faisceau d'électrons d'intense énergie. Il a été démontré que la génération des radicaux supplémentaires tels que le radical sulfate (SO4•−) et le radical hydroxyle par les réactions radicalaires entre l'ion persulfate, le peroxyde d'hydrogène et l'électron hydraté respectivement, am
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Varmenot, Nicolas. "Processus d'oxydation des sulfures organiques par le radical hydroxyle : influence du groupement S-acétyle." Paris 5, 2001. http://www.theses.fr/2001PA05S019.

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Les sulfures organiques exerçant d'importantes fonctions biologiques dans l'organisme sont très sensibles à l'agression des espèces activées de l'oxygène. L'étude des processus d'oxydation de ces composés est essentielle afin de mieux comprendre les mécanismes d'attaque et de réparation des systèmes biologiques soumis au stress oxydant. Du fait de l'influence déterminante des groupements chimiques avoisinant l'atome de soufre sur les mécanismes d'oxydation des molécules soufrées, nous nous sommes proposés dans ce travail de comprendre le rôle de la présence du groupement carbonyle (-C=O), en p
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Demougeot, Céline. "Etude de la toxicité cérébrale du fer et évaluation du N-Acétyl-L-aspartate comme marqueur biochimique de la mort neuronale : application à l'ischémie cérébrale." Dijon, 2001. http://www.theses.fr/2001DIJOPE02.

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Nous avons étudie chez le rat les effets d'une charge cérébrale en fer libre. Elle a été induite in vitro par exposition de coupes cérébrales a un complexe liposoluble ou hydrosoluble de fer sérique, et in vivo par injection striatale des mêmes complexes. Les résultats montrent que la production de radicaux hydroxyles par les coupes cérébrales est plus importante en présence du complexe liposoluble de fer et que les dommages histologiques secondaires a l'injection intracérébrale de fer dépendent de la vitesse a laquelle la teneur intracellulaire en fer libre augmente. De plus, nous montrons qu
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Abila, Paul-André. "Application de la spectroscopie moléculaire au diagnostic d'un plasma inductif d'argon." Lyon, INSA, 1989. http://www.theses.fr/1989ISAL0074.

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Les techniques de spectroscopie moléculaire n'ont été que peu utilisées pour le diagnostic dans les plasmas d'argon induits par haute fréquence à la pression atmosphérique comme la plupart des molécules y sont dissociées. Néanmoins, certaines y sont observables, elles la molécule OH. Les températures déduites des spectres de rotation-vibration de OH sont plus faibles (maximum voisin de 4000 K) que celles déduites du spectre d'autres molécules ( N2 par exemple, environ 7000 K) ou des spectres atomiques ( 4500 à 7000 K) , dans les mêmes conditions. Ceci semble lié à la stabilité thermique de la
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El, Omar Abdel Karim. "Études des réactions primaires en solutions par la radiolyse pulsée picoseconde." Phd thesis, Université Paris Sud - Paris XI, 2013. http://tel.archives-ouvertes.fr/tel-00931405.

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Après la découverte des rayonnements ionisants et leurs effets chimiques, il était important d'étudier et de comprendre les mécanismes de formations des radicaux libres et des produits moléculaires caractérisés par leurs courtes durées de vie. Ceci a encouragé les groupes de recherches à développer leurs outils pour qu'ils puissent réaliser ces études. De nos jours la radiolyse impulsionnelle se manifeste comme un outil fondamental permettant de sonder les effets chimiques ainsi que les mécanismes réactionnels dans le milieu étudié.Le laboratoire de Chimie Physique d'Orsay " LCP " est un labor
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Brosse, Fabien. "Influence de la couche limite convective sur la réactivité chimique en Afrique de l'Ouest." Thesis, Toulouse 3, 2017. http://www.theses.fr/2017TOU30324/document.

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Cette thèse porte sur l'influence de la couche limite convective et nuageuse sur la réactivité chimique en Afrique de l'Ouest. Pour répondre à cette question, des simulations à haute résolution (50m) sont réalisées sur le modèle atmosphérique Méso-NH couplé à un mécanisme chimique détaillé représentant la chimie gazeuse et aqueuse. Cette échelle spatiale permet de représenter explicitement les caractéristiques spatiales et temporelles des structures turbulentes. Les thermiques en couche limite sont identifiés à l'aide d'un échantillonnage conditionnel basé sur l'utilisation d'un traceur passif
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Oppilliart, Sophie. "Etude par échange isotopique du radical tyrosyle en solution et dans la catalase bovine." Phd thesis, Université Paris Sud - Paris XI, 2007. http://tel.archives-ouvertes.fr/tel-00361211.

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Lors de la dégradation du peroxyde d'hydrogène en eau et dioxygène catalysée par les hémoenzymes à fer de type catalase et peroxydase, il se forme à l'échelle de la milliseconde un intermédiaire réactionnel radicalaire porté par la porphyrine. Dans le cas de l'enzyme modèle utilisée, la catalase de foie de bœuf, il a été montré par des études de spectroscopie RPE que ce radical est ensuite délocalisé sur un résidu tyrosyle de la chaîne polypeptidique. A ce jour, on ne connaît pas l'exacte localisation du résidu impliqué, donc le rôle de ce site d'oxydation alternatif. <br />Par ailleurs, il a
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Lallement, Audrey. "Impact des processus photochimiques et biologiques sur la composition chimique du nuage." Thesis, Université Clermont Auvergne‎ (2017-2020), 2017. http://www.theses.fr/2017CLFAC066/document.

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Dans un contexte de réchauffement climatique, une compréhension des mécanismes atmosphériques influençant le bilan radiatif terrestre est nécessaire. Les nuages peuvent participer à un refroidissement mais des incertitudes demeurent sur ces systèmes qui sont encore mal connus (notamment la composition de leur fraction organique). Depuis toujours, seules les réactions chimiques et surtout celles radicalaires sont considérées comme importantes pour jouer sur la composition des nuages. Cependant la découverte de microorganismes métaboliquement actifs pose la question de leur rôle en tant que bioc
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Rabat, Hervé. "Utilisation du spectre UV du radical OH dans la métrologie des hautes températures des gaz chauds et des plasmas." Orléans, 2004. http://www.theses.fr/2004ORLE2050.

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La bibliographie présente l’étude du radical OH dans les flammes, puis une méthode de simulation de son spectre UV. La partie expérimentale concerne les études thermiques d’une flamme oxy-acétylénique et d’un panache de plasma d’argon par des méthodes spectroscopiques et interférométriques. Outre la validation de la simulation, elles montrent que la densité de OH tend avec la hauteur dans la flamme vers une répartition radiale gaussienne. Parallèlement, nous montrons que la température rotationnelle de OH reste, pour ces mêmes hauteurs, constante sur le diamètre de la flamme. La dernière parti
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Joshi, Prasad. "Isolation and reactivity of hydroxyl radical with astrochemically and atmospherically relevant species studied by Fourier transform infrared spectroscopy." Paris 6, 2012. http://www.theses.fr/2012PA066092.

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Les radicaux OH jouent un rôle très important dans la chimie des milieux interstellaires. Dans la mesure où il s’agit d’espèces très réactives, l’isolation et la détection expérimentale de ces radicaux est délicate. Pourtant, cette étape est un prérequis nécessaire pour des études de réactivités qui pourraient s’avérer fondamentales dans de nombreux domaines, en particulier pour la chimie des milieux interstellaires et des atmosphères planétaires. Différents protocoles expérimentaux ont été utilisés pour former les radicaux OH. Dans un premier temps, de l’eau pure, à l’état gazeux, a été soumi
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Books on the topic "Hydroxyle radical"

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Edney, Edward. Hydroxyl radical rate constant intercomparison study. U.S. Environmental Protection Agency, Atmospheric Sciences Research Laboratory, 1987.

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Crosley, David R. Local measurement of tropospheric HOx: Summary of a workshop held at SRI International, Menlo Park, California, March 23-26, 1992. Langley Research Center, 1994.

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Sharkey, Paul. Kinetics of hydroxyl radical reactions at low temperatures. University of Birmingham, 1994.

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United States. National Aeronautics and Space Administration., ed. Spectroscopic study of combustion diagnostics on hydroxyl radicals: Final research report. The University of Alabama in Huntsville, 1990.

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B, DeMore William, and United States. National Aeronautics and Space Administration., eds. Temperature-dependent rate constants and substituent effects for the reactions of hydroxyl radicals with three partially fluorinated ethers. 2nd ed. National Aeronautics and Space Administration, 1995.

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B, DeMore William, and United States. National Aeronautics and Space Administration., eds. Temperature-dependent rate constants and substituent effects for the reactions of hydroxyl radicals with three partially fluorinated ethers. 2nd ed. National Aeronautics and Space Administration, 1995.

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H, Phillips Donald, and Langley Research Center, eds. An ab initio investigation of possible intermediates in the reaction of hydroxy and hydroperoxyl radicals. National Aeronautics and Space Administration, Langley Research Center, 1985.

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Lacheur, Richard M. Le. Reactions of ozone and hydroxyl radicals with amino acids. The Foundation and American Water Works Association, 1995.

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Burnett, Elizabeth Beaver. Periodic behaviors in the observed vertical column abundances of atmospheric hydroxyl. Florida Atlantic University, 1989.

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Carter, Campbell D. Saturated fluorescence measurements of the hydroxyl radical in laminar high-pressure flames. Purdue University, 1990.

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Book chapters on the topic "Hydroxyle radical"

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Irvine, William M. "Hydroxyl Radical." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1810.

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Irvine, William M. "Hydroxyl Radical." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1810.

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Irvine, William M. "Hydroxyl Radical." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1810-4.

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Bell, David M., Manuela Cirtog, Jean-François Doussin, et al. "Preparation of Experiments: Addition and In Situ Production of Trace Gases and Oxidants in the Gas Phase." In A Practical Guide to Atmospheric Simulation Chambers. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-22277-1_4.

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AbstractPreparation of the air mixture used in chamber experiments requires typically the injection of trace gases into a bath gas. In this chapter, recommendations and standard protocols are given to achieve quantitative injections of gaseous, liquid or solid species. Various methods to produce ozone, nitrate radicals and hydroxyl radicals are discussed. Short-lived oxidants need to be produced during the experiment inside the chamber from pre-cursor species. Because highly reactive oxidants like hydroxyl radicals are challenging to detect an alternative method for the quantification of radic
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O'Brien, Robert J., and Thomas M. Hard. "Tropospheric Hydroxyl Radical." In Advances in Chemistry. American Chemical Society, 1993. http://dx.doi.org/10.1021/ba-1993-0232.ch012.

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Irvine, William M. "Hydroxyl Radical (OH)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1810.

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Hoffman, M. Z. "Of Hydroxyl Radicals." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145302.ch107.

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McKenzie, Thomas G., Amin Reyhani, Mitchell D. Nothling, and Greg G. Qiao. "Hydroxyl Radical Activated RAFT Polymerization." In ACS Symposium Series. American Chemical Society, 2018. http://dx.doi.org/10.1021/bk-2018-1284.ch014.

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Kiran, Tugba Raika, and Aysun Bay Karabulut. "Free Radicals and Antioxidants in Diabetics." In Current Multidisciplinary Approach to Diabetes Mellitus Occurrence Mechanism. Nobel Tip Kitabevleri, 2023. http://dx.doi.org/10.69860/nobel.9786053359104.5.

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In diabetics, there is an imbalance between free radicals and antioxidants, leading to oxidative stress, a condition characterized by increased production of reactive oxygen species (ROS) and impaired antioxidant defenses. Free radicals, such as superoxide anion (O2•−), hydroxyl radical (•OH), and hydrogen peroxide (H2O2), are generated as by-products of normal cellular metabolism and play a role in cell signaling and immune response. However, excessive ROS production in diabetes, exacerbated by hyperglycemia and insulin resistance, overwhelms antioxidant defenses, which include enzymatic anti
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Jagannathan, Indu, and Jeffrey J. Hayes. "Hydroxyl Radical Footprinting of Protein-DNA Complexes." In Methods in Molecular Biology™. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-015-1_5.

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Conference papers on the topic "Hydroxyle radical"

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Schweizer, Christian, Matthew Hay, Chad V. Mashuga, and Waruna D. Kulatilaka. "OH-PLIF Diagnostics of Niacin Dust Flames." In Laser Applications to Chemical, Security and Environmental Analysis. Optica Publishing Group, 2024. https://doi.org/10.1364/lacsea.2024.lw3e.5.

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Hydroxyl radical planar laser-induced fluorescence (OH-PLIF) imaging is implemented to characterize the flame structure of burning niacin dust clouds. The flame morphology is analyzed using two-dimensional flame area and curvature measurements.
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Mooney, C. E., L. C. Anderson, and J. H. Lunsford. "Formation and desorption of hydroxyl radicals during Pt-catalyzed oxidation." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.thii4.

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Heterogeneously catalyzed reactions often involve reactive radical intermediates that are produced on the surface and subsequently desorb into the gas phase. In this work, laser-induced fluorescence (LIF) has been used to measure OH radical desorption from a catalytically active polycrystalline platinum wire during the oxidation of methane and hydrogen. The temperature range of the wire was 900 K to 1300 K, and reactant partial pressures were kept between 1 and 20 mtorr to minimze any gasphase reactions. Under these conditions the surface reactions and energetics involving the hydroxyl radical
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King, Matthew, and Raoul Kopelman. "Development of a hydroxyl radical nanoprobe." In International Symposium on Biomedical Optics, edited by Gerald E. Cohn. SPIE, 2002. http://dx.doi.org/10.1117/12.469776.

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Zhao, Yi Yi, Mark P. Wilson, Tao Wang, Igor V. Timoshkin, and Scott J. MacGregor. "Hydroxyl radical production in DC streamer discharge." In 2015 IEEE Pulsed Power Conference (PPC). IEEE, 2015. http://dx.doi.org/10.1109/ppc.2015.7296962.

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Dong, Fang, Qinzhao Xue, Jingli Liu, Zhanyong Guo, Hongmao Zhong, and Huili Sun. "The Influence of Amino and Hydroxyl of Chitosan on Hydroxyl Radical Scavenging Activity." In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163624.

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Sears, Trevor J., H. E. Radford, and Mary Ann Moore. "b-Dipole Transitions in X ˜ 2A' t-HOCO Observed by FIR Laser Magnetic Resonance." In High Resolution Spectroscopy. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/hrs.1993.thb1.

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The HOCO radical is crucially important in combustion chemistry as the intermediate in the reaction between hydroxyl radicals and carbon monoxide. Studies of the temperature dependence of the rate constant for this reaction implied the existence of the radical intermediate1 but only very recently was HOCO detected in the gas phase2,3. Both the infrared spectrum3, which is due to the perturbed C=O stretching fundamental (v2), and the observed rotational spectrum2 consist only of a-dipole transitions. Such transitions obey the selection rule ΔKa = 0 in this near prolate top rotor and as such con
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Zhang, Fenghua, Changzheng Zhou, and Chuanlin Tang. "Capacity of Hydroxyl Radical Produced by Choking Cavitator." In The 3rd International Conference on Machinery, Materials Science and Energy Engineering (ICMMSEE 2015). WORLD SCIENTIFIC, 2015. http://dx.doi.org/10.1142/9789814719391_0024.

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Khalil Hasan, Ahmed E., and Ashwani K. Gupta. "Hydroxyl Radical Distribution under Colorless Distributed Combustion Conditions." In 52nd Aerospace Sciences Meeting. American Institute of Aeronautics and Astronautics, 2014. http://dx.doi.org/10.2514/6.2014-0459.

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DeMore, William B. "Rates of hydroxyl radical reactions with some HFCs." In Environmental Sensing '92, edited by Harold I. Schiff and Ulrich Platt. SPIE, 1993. http://dx.doi.org/10.1117/12.140207.

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Han, Ruixia, Gang Li, and Yong-Guan Zhu. "Humic Substances Affect Iron-Driven Hydroxyl Radical Production." In Goldschmidt2023. European Association of Geochemistry, 2023. http://dx.doi.org/10.7185/gold2023.15484.

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Reports on the topic "Hydroxyle radical"

1

Lee, Y., H. Pennline, and J. Markussen. Flue gas cleanup with hydroxyl radical reactions. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7163736.

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2

Chan, Cornelius. Laser induced hydroxyl radical fluoresence at atmospheric pressure. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.69.

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3

Lester, Marsha I. Quenching Dynamics of Electronically Excited Hydroxyl Radicals. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada482242.

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Calidonna, Sheryl E., and William R. Bradley. The Hydroxyl Radical Reaction Rate Constant and Products of Dimethyl Succinate. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada489770.

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Peterman, Dean R., Gregory P. Horne, Jamie M. Gleason, Anneka J. Miller, and Stephen P. Mezyk. Determine rate of reaction of hydroxyl radical with carboxylic acids and polyaminocarboxylates. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1483694.

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Lester, M. I. Spectroscopy and reaction dynamics of collision complexes containing hydroxyl radicals. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5710534.

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Peak, J. G., T. Ito, M. J. Peak, and F. T. Robb. DNA damage produced by exposure of supercoiled plasmid DNA to high- and low-LET ionizing radiation: Effects of hydroxyl radical quenchers. DNA breakage, neutrons, OH radicals. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10172487.

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Cohen, N. A shock tube study of the reactions of the hydroxyl radical with combustion species. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5573201.

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Atherton, C. S. Predicting tropospheric ozone and hydroxyl radical in a global, three-dimensional, chemistry, transport, and deposition model. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/130611.

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Cohen, N. A shock tube study of the reactions of the hydroxyl radical with combustion species and pollutants. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6645854.

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